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AMBU NEUROLINE SINGLE PATIENT EEG/EP CUP ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K032278
510(k) Type
Traditional
Applicant
AMBU, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/2004
Days to Decision
225 days
Submission Type
Statement

AMBU NEUROLINE SINGLE PATIENT EEG/EP CUP ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K032278
510(k) Type
Traditional
Applicant
AMBU, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/2004
Days to Decision
225 days
Submission Type
Statement